1. Surgalign Holdings received FDA 510(k) clearance for its Holo Portal surgical system for lumbar spine surgeries. Holo Portal is described as the first artificial intelligence-driven augmented reality guidance system for spine surgery.
2. Stryker’s Q guidance system received FDA 510(k) clearance for spine surgery applications. The Q system is designed for advanced surgical planning and intraoperative guidance for open or percutaneous computer-assisted surgery.
3. VisAR, an augmented reality surgical guidance system, received FDA clearance for intraoperative spine surgery. The system transforms imaging data into a 3D hologram that is visible and superimposed on the patient.
4. MicroPort Navibot has received FDA 510(k) clearance of its first robot-assisted platform for orthopedic use. The Skywalker system will initially be used for total knee replacements and is compatible with the Evolution medial-pivot total knee system.
5. Point Robotics MedTech’s Point Kinguide system received FDA 510(k) clearance. It is Taiwan’s first FDA-cleared surgical robot and the first handheld robot with a parallel manipulator for orthopedics.
